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CompletedNCT07441551Updated Mar 2, 2026

Ergonomic Risk and Musculoskeletal Characteristics in Industrial Workers

An observational study in Ergonomic Risk and Work-related Musculoskeletal Characteristics in Blue- and White-collar Workers, sponsored by Istinye University. Completed at 1 site in Turkey (Türkiye). Open to participants aged 18 Years to 65 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-03-02.

Sponsored by Istinye University · Observational

Study type
Observational
Model
Other
Time perspective
Cross-sectional
Enrollment
40
Ages
18 Years to 65 Years
Sex
All
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Study summary

Musculoskeletal disorders (MSDs) are among the most common occupational health problems and are closely associated with ergonomic risk factors in the workplace. Different occupational roles expose workers to distinct biomechanical and postural demands, which may influence musculoskeletal health in different ways. Field-based (blue-collar) work is typically characterized by physical workload and repetitive movements, whereas office-based (white-collar) work mainly involves prolonged sitting and static postures.

This cross-sectional comparative study aims to evaluate and compare musculoskeletal characteristics and ergonomic risk levels between blue-collar and white-collar workers employed in the same industrial setting. Full-time employees aged 18-65 years who have been working in the same factory for at least two years are included.

Outcomes include muscle strength, joint range of motion, ergonomic risk assessed using the Rapid Entire Body Assessment (REBA), musculoskeletal complaints, body awareness, health-related quality of life, and anxiety levels. Objective measurements and validated self-report questionnaires are used.

Following baseline assessment, individualized ergonomic and exercise-based recommendations are provided as part of a workplace health promotion approach. Participant satisfaction and perceived ergonomic awareness are descriptively evaluated after eight weeks. The findings aim to support occupation-specific ergonomic risk assessment and preventive strategies in industrial work environments.

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Conditions studied

  • Ergonomic Risk and Work-related Musculoskeletal Characteristics in Blue- and White-collar Workers

Keywords

  • Occupational health
  • Ergonomic risk
  • Musculoskeletal characteristics
  • Industrial workers
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In context

Lead sponsor

Istinye University is the lead sponsor of 207 studies on the registry; 88 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Study Population Description

The study population consists of full-time blue-collar and white-collar employees aged 18 to 65 years who are working in the same industrial (factory) setting. Participants have been employed in the factory for at least two consecutive years and have maintained their current job position for a minimum of one year. The population represents actively working adults exposed to different occupational ergonomic demands within the same organizational environment.

Inclusion criteria

  • Aged between 18 and 65 years
  • Employed in the same factory for at least two consecutive years
  • Actively working in either field-based (blue-collar) or office-based (white-collar) positions
  • Full-time employment status
  • Maintained the current job position for at least one year prior to assessment
  • Willingness to participate and provision of written informed consent

Exclusion criteria

Exclusion Criteria

  • Presence of a diagnosed cardiovascular condition contraindicating physical activity
  • Orthopedic surgery within the previous 12 months
  • Presence of a neurological disorder affecting motor performance
  • Acute musculoskeletal injury within the previous 3 months
  • Currently receiving structured physiotherapy or rehabilitation for musculoskeletal conditions
  • Pregnancy at the time of assessment
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Study design

Observational model
Other
Time perspective
Cross-sectional
Enrollment
40 participants (actual)
Patient registry
No

Groups and cohorts

  • Industrial Blue-Collar Workers

    This cohort includes full-time field-based employees working in physically demanding tasks within an industrial (factory) setting. Participants are primarily involved in manual labor, equipment handling, repetitive movements, and activities requiring dynamic postures. No experimental intervention is applied. Following baseline assessment, participants receive individualized ergonomic and exercise-based recommendations as part of a workplace health promotion initiative.

    Other: Workplace Ergonomic and Exercise Education

  • Industrial White-Collar Workers

    This cohort includes full-time office-based employees working in administrative and desk-based roles within the same industrial setting. Participants are primarily exposed to prolonged sitting, static working postures, and computer-based tasks. No experimental intervention is applied. Following baseline assessment, participants receive individualized ergonomic and exercise-based recommendations as part of a workplace health promotion initiative.

    Other: Workplace Ergonomic and Exercise Education

Interventions

  • OtherWorkplace Ergonomic and Exercise Education

    This intervention consists of individualized ergonomic and exercise-based recommendations provided following assessment. The content includes education on optimal working postures, workstation and task-related ergonomic principles, avoidance of prolonged static positions, safe manual handling techniques, and brief workplace-appropriate exercises aimed at promoting musculoskeletal health. The recommendations are delivered as part of a workplace health promotion and awareness approach and are not designed as a therapeutic or experimental intervention. No objective outcome-based effectiveness analysis is conducted.

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What researchers measure

Primary outcomes

  1. Joint Range of Motion

    Active joint range of motion (ROM) of the cervical spine, lumbar spine, and upper and lower extremities was measured using a universal goniometer (Hawker et al., 2011).

    Time frame: Baseline (single time point)

  2. Muscle Strength

    Hand grip strength was measured using a Jamar hand dynamometer, positioned according to the recommendations of the American Society of Hand Therapists (Mathiowetz et al., 1985). Isometric muscle strength of the deltoid, biceps brachii, triceps brachii, quadriceps, and hamstring muscle groups was assessed using a Lafayette handheld dynamometer (Mentiplay et al., 2015). Three maximal contraction trials were performed for each muscle group and hand grip strength, and the highest value obtained was recorded.

    Time frame: Baseline (single time point)

  3. Muscle Flexibility

    Lumbar extensor, hamstring, and gastrosoleus muscle flexibility were evaluated using the sit-and-reach test. The distance between the middle fingertip and the testing surface was recorded in centimeters (Otman et al., 2003).

    Time frame: Baseline (single time point)

Secondary outcomes

  1. Musculoskeletal Complaints

    Musculoskeletal symptoms were assessed using the Cornell Musculoskeletal Discomfort Questionnaire (CMDQ), a validated self-report instrument that evaluates the presence, frequency, and severity of musculoskeletal discomfort across multiple body regions. The questionnaire also captures the extent to which discomfort interferes with work performance. Scores are calculated based on frequency, severity, and work interference multipliers, allowing region-specific and total discomfort scores to be derived. Higher scores indicate greater musculoskeletal burden (Hedge et al., 1999). The Turkish version has demonstrated established validity and reliability (Erdinc et al., 2011). In the statistical analyses, the total CMDQ score, reflecting overall musculoskeletal discomfort burden, was used.

    Time frame: Baseline (single time point)

  2. Ergonomic Risk Assessment

    Ergonomic Risk Assessment: Ergonomic risk was evaluated using the Rapid Entire Body Assessment (REBA) method, an observational tool designed to assess whole-body postural risk associated with work tasks. REBA systematically scores trunk, neck, leg, and upper extremity positions, as well as load/force and coupling factors, generating a composite score that categorizes ergonomic risk into different action levels. Higher REBA scores indicate greater postural risk and the need for more urgent ergonomic intervention. Both static and dynamic working postures were directly observed and analyzed in the actual workplace environment. Observations were conducted by the same trained assessor to ensure consistency (Hignett \& McAtamney, 2000\[HÇ).

    Time frame: Baseline (single time point)

  3. Quality of Life Assessment

    Health-related quality of life was measured using the Short Form-36 (SF-36), a widely used generic instrument consisting of eight subdomains: physical functioning, role limitations due to physical health, bodily pain, general health perception, vitality, social functioning, role limitations due to emotional problems, and mental health. Subscale scores range from 0 to 100, with higher scores representing better perceived health status (Ware \& Sherbourne 1992). The Turkish version has demonstrated established validity and reliability (Koçyiğit et al., 1999).

    Time frame: Baseline (single time point)

  4. Anxiety Assessment

    Anxiety levels were assessed using the Beck Anxiety Inventory (BAI), a 21-item self-report questionnaire designed to measure the severity of anxiety symptoms. Each item is rated on a 4-point Likert scale (0-3), yielding a total score ranging from 0 to 63. Higher scores reflect greater anxiety severity (Beck et al., 1988). The Turkish version has demonstrated established validity and reliability (Ulusoy et al., 1998). The instrument has been widely used in both clinical and occupational populations.

    Time frame: Baseline (single time point)

  5. Body Awareness Assessment

    Body awareness was evaluated using the Body Awareness Questionnaire (BAQ), which measures an individual's sensitivity to normal bodily processes and internal physiological signals. The scale includes items rated on a Likert-type format, with higher total scores indicating greater body awareness (Shields et al., 1989). The Turkish version has demonstrated established validity and reliability (Karaca et al., 2021). This construct is particularly relevant in occupational settings, as heightened body awareness may influence early recognition of musculoskeletal strain and adaptive behavior

    Time frame: Baseline (single time point)

  6. Evaluation of Satisfaction and Awareness

    A structured questionnaire was developed to assess participants' satisfaction with the educational components and perceived awareness. Participants rated their satisfaction with posture education, ergonomic training, exercise instruction, and information regarding musculoskeletal conditions on a 0-5 scale. Baseline knowledge regarding ergonomics, work posture, workstation organization, and preventive exercises was assessed prior to education. The same items were re-administered after eight weeks to evaluate perceived changes in awareness. The questionnaire included items related to recognition of potential musculoskeletal risks, ability to identify appropriate working postures, knowledge of ergonomic adjustments, and understanding of preventive exercises. This evaluation aimed to describe perceived satisfaction and awareness changes rather than to determine objective clinical effectiveness.

    Time frame: 8 weeks after baseline assessment

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Study locations

1 site
  • İstinye Üniversitesi
    Istanbul, Turkey (Türkiye)
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 2, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07441551
Lead sponsor
Istinye University
Responsible party
Sponsor
First posted
Mar 2, 2026
Start date
Apr 15, 2025
Primary completion
Dec 30, 2025
Completion
Jan 30, 2026
Last update
Mar 2, 2026

Study contacts

Elif Cantürk, MS
study chair · Istinye University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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